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Diagnosis of Frontotemporal Dementia

Digital illustration of brain highlighting frontotemporal lobe damage

A futuristic brain scan illustration showing damage in the frontotemporal region, commonly associated with behavioural and cognitive decline in frontotemporal dementia

Diagnosis of Frontotemporal Dementia

The diagnosis of frontotemporal dementia can be challenging due to the wide variety of symptoms and the fact that frontotemporal dementia often mimics psychiatric disorders or other forms of dementia. Accurate and early diagnosis is essential to ensure appropriate treatment, planning, and support for the individual and their family.

Clinical Evaluation

The diagnostic process begins with:

A detailed history of symptoms, including changes in behaviour, language, or movement

Information from close family members or caregivers, who may notice changes the individual doesn’t

Neurological and cognitive tests, to assess memory, reasoning, speech, and behaviour patterns

Because early-stage FTD doesn’t usually affect short-term memory, standard dementia screening tools may not always detect it.

Brain Imaging

To confirm the diagnosis and rule out other causes, doctors may order imaging tests such as:

MRI (Magnetic Resonance Imaging) – can reveal shrinkage in the frontal and temporal lobes

CT scan – may show structural changes in the brain

PET or SPECT scans – show how the brain is functioning and highlight areas of reduced activity, even before major shrinkage is visible

These scans help differentiate FTD from other conditions like Alzheimer’s disease or vascular dementia.

Neuropsychological Testing

A neuropsychologist may carry out:

Detailed assessments of speech, language, and executive function

Tests to evaluate the ability to plan, organise, or interpret social cues

Emotional recognition tests, particularly for individuals with behavioural symptoms

These tools help identify specific deficits that align with different subtypes of FTD.

Blood Tests and Genetic Screening

While there is no blood test that confirms FTD, doctors may use blood tests to:

Rule out other medical conditions, such as thyroid problems, infections, or vitamin deficiencies

In inherited cases, genetic testing may be offered to identify mutations in genes like MAPT, GRN, or C9orf72

Genetic counselling is strongly recommended before and after testing.

Differential Diagnosis

FTD is often misdiagnosed as:

Depression or bipolar disorder

Alzheimer’s disease

Autism spectrum disorders, particularly in younger adults

A team approach involving neurologists, psychiatrists, and speech therapists often leads to more accurate results.

Diagnosis of Frontotemporal Dementia

A confirmed diagnosis of frontotemporal dementia allows families to access care resources early, plan for the future, and participate in research or clinical trials if appropriate.

[Next: Treatment of Frontotemporal Dementia →]

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